The invention relates generally to a small volume pipet, or micropipet. More particularly, the invention relates to a pipet for aliquoting small volumes of a biological fluid sample.
Measuring concentrations of administered drugs and their metabolites in biological fluids, such as whole blood, plasma and serum, is important to understanding the efficacy and toxicological effects of the drugs. Typical clinical studies require handling and processing large numbers of biological fluid samples at low temperature with special care. Dried spot sampling is an alternative practice that is based on collection of small volumes (e.g., several microliters or less) of biological fluids as dried spots. For example, dried blood spot (DBS) sampling involves the collection of small volumes of blood onto a carrier medium. Samples are reconstituted and analyzed, for example, in a liquid chromatography-mass spectrometry assay.
Dried sample spot processing can be performed in multiple ways. Samples are reconstituted from the dried spots using suitable solvents during an extraction process. In one procedure, a small disc is punched from the DBS sample carrier (e.g., DBS card). Examples of this process are described in PCT Patent Publication No. PCT/US2013/043562, titled “Solid Phase Extraction Device for Dried Sample Cards. The punch step functions as a volume aliquoting of the DBS. A precise sample volume may not be obtained under certain conditions, such as when the subject hematocrit deviates from a normal value. In some instances, the punched disc includes only a small portion of the collected sample and much of the collected sample is therefore wasted. In some implementations, the punching step is a manual procedure that serves as a bottleneck for the analytical procedure.
Whole spot elution is an alternative to the punch procedure. The elution process is described, for example, in U.S. patent application Ser. No. 13/698,164, titled “Apparatus and Methods for Preparation and Analysis of Dried Samples of a Biological Fluid,” the contents of which are incorporated by reference herein.
The whole-spot extraction and elution procedures require precision in the sample spotting process. Any inaccuracy in the volume of sample fluid applied to the dried sample carrier can result in inaccurate results from subsequent analytical measurements.
Delivering a small volume of a biological fluid, such as blood or plasma, is challenging due to the high viscosity of the fluid. For example, the volume of a droplet of blood can be a few hundred microliters. In some analytical applications, it is desirable to utilize smaller volumes of blood, for example, as small as 5 microliters (μl) or less. Pipets are often used to collect small volume samples of biological fluids. A conventional pipet can fail to aspirate the desired sample volume. When dispensing the collected fluid from the pipet to a sample carrier, a significant amount of the collected fluid may be left behind at the tip of the pipet.
A sample collection capillary, such as a blood collection capillary, can be used to acquire a fluid sample and dispense the sample to a dried sample carrier. Sample collection capillaries are commonly in the form of a disposable glass tube. The tube may have a single volume marking; however, the tube generally cannot collect and dispense a quantitative volume of sample. Moreover, sample collection capillaries are not suitable for dispensing the collected sample in multiple aliquots. Thus sample collection capillaries are not practical for use with dried sample carriers having multiple collection regions.
In one aspect, the invention features a pipet that includes a capillary tube having a bore, a plunger, a plug and a plunger stop mechanism. The plunger has a shaft with a first end disposed in the bore of the capillary tube and a second end opposite the first end configured for depressing by a user. The plug is disposed on the shaft of the plunger inside the bore of the capillary tube and is in slidable engagement with a bore surface to provide a seal against the bore surface. The plunger stop mechanism is in cooperative engagement with the shaft of the plunger to limit movement of the shaft in an axial direction to equal incremental distances.
In another aspect, the invention features a pipet that includes a capillary tube having a bore, a plunger, a plug and a dispensing stage. The plunger has a shaft with a first end disposed in the bore of the capillary tube and a second end that is opposite the first end and configured for depressing by a user. The plug is disposed on the shaft of the plunger inside the bore of the capillary tube and is in slidable engagement with a bore surface to provide a seal against the bore surface. The dispensing stage has a cylindrical shape and surrounds a first portion of a length of the capillary tube. The dispensing stage has an end configured to engage a surface of a dispensing structure having an opening so that a second portion of the length of the capillary tube extends through the opening by a predetermined distance.
The above and further advantages of this invention may be better understood by referring to the following description in conjunction with the accompanying drawings, in which like reference numerals indicate like elements and features in the various figures. For clarity, not every element may be labeled in every figure. The drawings are not necessarily to scale, emphasis instead being placed upon illustrating the principles of the invention.
Reference in the specification to “one embodiment” or “an embodiment” means that a particular, feature, structure or characteristic described in connection with the embodiment is included in at least one embodiment of the teaching. References to a particular embodiment within the specification do not necessarily all refer to the same embodiment.
The present teaching will now be described in more detail with reference to exemplary embodiments thereof as shown in the accompanying drawings. While the present teaching is described in conjunction with various embodiments and examples, it is not intended that the present teaching be limited to such embodiments. On the contrary, the present teaching encompasses various alternatives, modifications and equivalents, as will be appreciated by those of skill in the art. Those of ordinary skill having access to the teaching herein will recognize additional implementations, modifications and embodiments, as well as other fields of use, which are within the scope of the present disclosure as described herein.
The following terminology is used in accordance with the associated definitions. The term “pipet” means a device for transporting a volume of a liquid. A “micropipet” refers to a pipet that can dispense a collected fluid ranging from a volume of less than one microliter (μl) to more than 1,000 μl. Although various embodiments are described herein as “micropipets,” “pipet” embodiments having similar construction can accommodate greater fluid volumes. In some embodiments, the pipet is described for use in acquiring and dispensing blood samples but it should be recognized that the pipet may be used to acquire and deliver aliquots of other biological fluids and fluids in general.
In brief overview, the invention relates to a pipet, or micropipet, that can be used to dispense multiple aliquots of an acquired fluid sample, such as a biological fluid sample. The pipet includes a capillary tube and a plunger. The capillary tube is filled with the fluid sample by capillary force or by withdrawing the plunger from the capillary tube to create a vacuum to draw in the fluid. A plunger stop mechanism having multiple stop positions allows the plunger to move further into the capillary tube through incremental axial distances of equal value. The plunger stop mechanism enables the pipet to dispense portions of the acquired volume of fluid with the dispensed portions having equal volumes.
Advantageously, the micropipet can be fabricated at low cost. Preferably, the micropipet is used as a disposable device that is discarded after a single use. The micropipet may be provided to users along with a sample collection device. By way of example, the micropipet is suitable as part of a kit that also contains a DBS card having multiple collection regions. The user uses the micropipet to acquire a single blood sample and subsequently aliquots the acquired sample onto the collection regions of the sample collection device with each collection region receiving the same volume of blood.
During a preferred dispensing procedure, the user depresses the plunger through the controlled incremental distance and a fluid droplet is formed at the end, or tip, of the capillary tube. The fluid droplet is allowed to touch the surface of the collection media. The micropipet can include an optional dispensing stage that maintains a predetermined separation between the tip of the micropipet and a surface of a sample collection device when the fluid is dispensed. The separation distance is selected to allow the droplet to touch the collection media surface without allowing the tip of the capillary tube to come in contact with the collection media. Thus wicking of fluid present inside the capillary tube into the collection media is avoided. Wicking, if allowed to occur, can draw additional fluid from the capillary tube and thus reduce the volume accuracy of the dispensed fluid.
The micropipet 10 also includes a plunger multi-stop mechanism to enable easy incremental motion of the plunger into the capillary tube 14 through equal distances d. The illustrated plunger stop mechanism is in the form of a spring-loaded plunger stop 34. One end of the plunger stop 34 is secured to the outer surface of the capillary tube 14. The other end of the plunger stop 34 has a tooth-like extension 38 shaped to engage one of the circumferential grooves 22 along the shaft 18. In other embodiments, the plunger multi-stop mechanism can have an alternative form as long as equal incremental plunger motions are achieved. For example, instead of circumferential grooves 22, the shaft can have saw-tooth variations in its radius arranged along the length of the shaft. The saw-tooth profile can be asymmetric to allow the extension 38 to easily pass over a saw-tooth profile as the plunger is inserted into the bore of the capillary tube 14 while preventing the shaft 18 from moving in the reverse direction.
To obtain a blood sample, the plunger is withdrawn from the capillary tube 14 until the plug 26 is near the end of the capillary tube 14 nearest to the plunger stop 34 so that the extension 38 “snaps into”, or engages, one of the grooves 22. Alternatively, the plunger is withdrawn further from the last groove 22 to create an internal volume larger than the desired sampling volume. The tip 42 of the capillary tube 14 is brought into contact with a source of blood so that a blood sample wicks up into the bore of the capillary tube 14 by capillary force. The blood source may be a patient or laboratory subject, or may be a container holding a previously-acquired blood sample. By way of a non-limiting numerical example, a capillary tube having an inner diameter of 0.033 in. can wick approximately 11 μl of blood when vertical. The volume of the blood sample that is acquired generally increases for orientations of the capillary tube that are increasingly more horizontal. The acquired volume can exceed 20 μl if the capillary tube is nearly horizontal.
To dispense the blood sample in the capillary tube 14, a user depresses the plunger so that the length of the shaft 18 inside the capillary tube 14 increases by the distance d and the extension 38 on the plunger stop 34 engages the next circumferential groove 22. Thus a small droplet of blood is dispensed at the tip 42 of the capillary tube 14.
For a whole-spot elution procedure, it is desirable to use spots obtained from approximately 5 μl of blood. If the volume of the acquired blood sample within the capillary tube 14 is substantially greater than 15 μl, the separations of the circumferential grooves 22 on the plunger shaft 18 can be selected to dispense three aliquots of 5 μl of blood.
It is common practice to run replicate samples in bioanalysis. Thus spotting collection devices with a “single stage” dispenser would require three dispensers for a single triplicate application; however, only one illustrated micropipet 10 is necessary for a single sampling (e.g., a single blood draw) and triplicate dispensing. In other embodiments, the number of aliquots that can be dispensed can be different. For example, a micropipet may be configured for four aliquots to allow for triplicate dispensing with a reserve aliquot for reanalysis of the sample at a later time. The illustrated micropipet 10 can be modified to dispense four aliquots by providing an additional circumferential groove 22 spaced a distance d from the first or last groove on the shaft 18.
In another embodiment of a micropipet 20, as shown in the partial side view of
To dispense fluid from the micropipet 20, the plunger is twisted (rotated) to move the extension 16 to one end of a circumferential groove segment 36B, then the plunger is depressed through a distance d to provide an aliquot. Additional twisting and depressing of the plunger through additional distances d allows for additional aliquots of equal volume to be dispensed.
Referring again to
A length L of the capillary tube 14 extends from the end of the case 54 which acts as part of a positioning mechanism to prevent the tip 42 of the capillary tube 14 from contacting the collection media. Referring to
To dispense aliquots of blood into a well 68, the micropipet 50 is maneuvered so that the capillary tube 14 extending from the case 54 passes through the corresponding opening 80 in the positioning cover 64. The end 56 of the case 54 comes into contact with the upper surface 88 of the positioning cover 64, thereby stopping the tip 42 of the capillary tube 14 at a distance Δ above the top of the collection media. The distance Δ is selected to allow the dispensed blood droplet at the tip 42 to come into contact with the upper surface 84 of the collection media while preventing the wicking problem described above if the tip 42 were to be in direct contact with the surface of the collection media.
Preferably the positioning cover 64 is fabricated from a transparent material so that the user can view the dispensed blood during the spotting process. The positioning cover 64 also functions as a protective layer. The openings 80 in the cover are preferably sealed with a thin protective media, such as plastic film, to protect the device 60 before spotting into the wells 68. At the time of spotting the seals are removed, or broken with the tip 42 of the capillary tube 14.
Although described above as a cylindrical case 54, in alternative embodiments the dispensing stage has a different form. For example, the dispensing stage can include any structure that extends radially from the outer surface of the capillary tube 14 at an axial position that achieves the desired separation distance Δ between the tip 42 of the capillary tube 14 and the upper surface 84 of the collection media.
In other embodiments, the micropipet includes a case that is configured for use with other types of collection devices, such as DBS cards. In one embodiment, a box-shaped positioning cover having an open bottom can be placed over the DBS card and properly positioned with respect to the card using alignment features. The top of the box-shaped cover has openings to pass the portion of the capillary tube 14 extending from the case 54.
The height of the box-shaped cover and the thickness of the wall having the openings are selected to achieve the desired offset Δ between the tip 42 of the capillary tube 14 and the upper surface of the collection media on the DBS card.
While the invention has been shown and described with reference to specific embodiments, it should be understood by those skilled in the art that various changes in form and detail may be made therein without departing from the spirit and scope of the invention as recited in the accompanying claims For example, various embodiments of the micropipet are described as dispensing three or four aliquots, it should be recognized that in other embodiments the micropipet can be configured to deliver other numbers of aliquots from a single sample collection.
This application claims the benefit of the earlier filing date of U.S. Provisional Patent Application No. 61/835,866, filed Jun. 17, 2013 and titled “Micropipet for Aliquoting Small Volumes of Liquid,” the entirety of which is incorporated herein by reference.
Filing Document | Filing Date | Country | Kind |
---|---|---|---|
PCT/US14/37074 | 5/7/2014 | WO | 00 |
Number | Date | Country | |
---|---|---|---|
61835866 | Jun 2013 | US |